Completing a Case Report Form SOP 351

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Overview

The aim of this Standard Operating Procedure SOP is to aid in the completion of CRFs used in clinical trials to collect data generated for a trial subject in accordance with the protocol during the course of their participation in a trial. They also ensure compliance with regulatory requirements such as that of the MHRA and as such may be audited or inspected

Categories
Clinical
Reference
Date Uploaded
26.10.2016
Date Review
23.08.2017
File Size
205Kb


Clinical Guidelines
This guideline has been approved by the Trust's Clinical Guidelines Assessment Panel as an aid to the diagnosis and management of relevant patients and clinical circumstances. Not every patient or situation fits neatly into a standard guideline scenario and the guideline must be interpreted and applied in practice in the light of prevailing clinical circumstances, the diagnostic and treatment options available and the professional judgement, knowledge and expertise of relevant clinicians. It is advised that the rationale for any departure from relevant guidance should be documented in the patient's case notes.
The Trust's guidelines are made publicly available as part of the collective endeavour to continuously improve the quality of healthcare through sharing medical experience and knowledge. The Trust accepts no responsibility for any misunderstanding or misapplication of this document.